Device recall

Z-2128-2023: Abiomed 14Fr Low Profile Introducer Set, Product Number 1000457

FDA device recall · Class II · Abiomed, Inc.

Key facts

Recall number (Z-number) Z-2128-2023
Recall event 92521
Product Abiomed 14Fr Low Profile Introducer Set, Product Number 1000457
Product code DYB
Recalling firm Abiomed, Inc.
Recall class Class II
Status Open, Classified
510(k) numbers K222113
FEI number 1220648

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)